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Synthesis, structures and properties of six lanthanide complexes based on a 2-(2-carboxyphenyl)imidazo(4,5-f)-(1,10)phenanthroline ligand

机译:基于2-(2-羧基苯基)咪唑(4,5-F) - (1,10)菲咯啉配体的六镧系元络合物的合成,结构和性质

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摘要

Six lanthanide complexes [Tb(2-NCP)(2)(NO3)](n) (1), [Eu(2-NCP)(2)(3-PYC)](n) (2), [Sm(2-NCP)(2)(3-PYC)](n) (3), [Eu(2-NCP)(SA)](n) (4), [Tb(2-NCP)(SA)](n) (5) and [Tb(2-NCP)(AA)](n) (6) (2-HNCP = 2-(2-carboxyphenyl) imidazo(4,5-f)-(1,10) phenanthroline, 3-HPYC = pyridine-3-carboxylic acid, H(2)SA = succinic acid, H(2)AA = adipic acid) have been synthesized by hydrothermal route, and the crystal structures were analyzed through elemental analysis, infrared spectroscopy, single crystal X-ray diffraction. Complexes 1 and 6 present two-dimensional (2D) layers, which are further connected to three-dimensional (3D) supramolecular architectures through C-H center dot center dot center dot pi interactions. Complexes 2 and 3 exhibit infinite one-dimensional chains. Finally, the neighboring chains are packed by C-H center dot center dot center dot pi interactions, giving rise to 3D supramolecular network. Complexes 4 and 5 display 2D layers, which are further extend to 3D supramolecular structures via C-H center dot center dot center dot O intermolecular hydrogen bonding. Six complexes possess good thermal stabilities, characteristic photoluminescence properties, and photocatalytic activities for the degradation of organic dyes under visible light irradiation. In addition, the complex 6 exhibits significantly enhanced photocatalytic activity for methylene blue, and the degradation rate could reach 81.2% in 370 min. Meanwhile trapping experiments indicated that the hole, center dot O-2(-) and center dot OH are the main activated species. Furthermore, by comparing the photoluminescent and photocatalytic mutation results of same metal complexes induced by interconversion of coligands, we confirm that the properties mutation induced by coligands is much obvious and controllable.
机译:六个镧系元络合物[TB(2-NCP)(2)(2)(NO 3)](N)(1),[EU(2-NCP)(2)(3-PYC)](N)(2),[SM( 2-NCP)(2)(3-PYC)](N)(3),[EU(2-NCP)(SA)](N)(N)(4),[TB(2-NCP)(SA)]( n)(5)和[Tb(2-NCP)(Aa)](N)(N)(6)(2-HNCP = 2-(2-羧基苯基)咪唑(4,5-F) - (1,10)菲咯啉,3-HPyC =吡啶-3-羧酸,H(2)SA =琥珀酸,H(2)AA =己二酸)已经通过水热途径合成,通过元素分析,红外光谱分析晶体结构,单晶X射线衍射。复合物1和6存在二维(2D)层,其通过C-H中心点中心点中心点PI相互作用进一步连接到三维(3D)超分子架构。复合物2和3表现出无限的一维链。最后,邻近的链条被C-H中心点中心点中心点PI相互作用包装,从而产生3D超分子网络。复合物4和5显示器2D层,其经由C-H中心点中心点中心点O分子间氢键进一步延伸到3D超分子结构。六个配合物具有良好的热稳定性,特征光致发光性能,以及用于在可见光照射下的有机染料的降解的光催化活性。此外,复合物6表现出显着增强的亚甲基光催化活性,降解速率在370分钟内可达到81.2%。同时捕获实验表明,孔,中心点O-2( - )和中心点OH是主要的活性物质。此外,通过比较通过Coligand的相互互连诱导的相同金属配合物的光致发光和光催化突变结果,我们证实Cooligands诱导的性质突变显而易见和可控。

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  • 来源
    《RSC Advances》 |2019年第6期|共11页
  • 作者单位

    Jilin Normal Univ Minist Educ Key Lab Preparat &

    Applicat Environm Friendly Mat Changchun 130103 Jilin Peoples R China;

    Jilin Normal Univ Minist Educ Key Lab Preparat &

    Applicat Environm Friendly Mat Changchun 130103 Jilin Peoples R China;

    Jilin Normal Univ Minist Educ Key Lab Preparat &

    Applicat Environm Friendly Mat Changchun 130103 Jilin Peoples R China;

    Jilin Normal Univ Minist Educ Key Lab Preparat &

    Applicat Environm Friendly Mat Changchun 130103 Jilin Peoples R China;

    Jilin Normal Univ Minist Educ Key Lab Preparat &

    Applicat Environm Friendly Mat Changchun 130103 Jilin Peoples R China;

    Jilin Normal Univ Minist Educ Key Lab Preparat &

    Applicat Environm Friendly Mat Changchun 130103 Jilin Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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